Linked Data
ClinVar Variation Id:
245986
dbSNP Id:
rs144874997
ExAC:
2:86459814 G / A
gnomAD v2:
2-86459814-G-A
gnomAD v3:
2-86232691-G-A
gnomAD v4:
2-86232691-G-A
COSMIC:
COSM1471360
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.86232691G>A , CM000664.2:g.86232691G>A | GRCh38 |
| NC_000002.11:g.86459814G>A , CM000664.1:g.86459814G>A | GRCh37 |
| NC_000002.10:g.86313325G>A | NCBI36 |
| NG_013037.1:g.110393C>T , LRG_713:g.110393C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643817.2:c.529C>T | ENSP00000495610.2:p.Arg177Trp | |
| ENST00000686220.1:c.448C>T | ENSP00000509904.1:p.Arg150Trp | |
| ENST00000688400.1:c.217C>T | ENSP00000510490.1:p.Arg73Trp | |
| ENST00000689156.1:c.418-15581C>T | ENSP00000509143.1:n.418-15581C>T | |
| ENST00000691093.1:c.349C>T | ENSP00000509465.1:p.Arg117Trp | |
| ENST00000691703.1:c.529C>T | ENSP00000508496.1:p.Arg177Trp | |
| ENST00000692664.1:c.379C>T | ENSP00000508656.1:p.Arg127Trp | |
| ENST00000693329.1:c.529C>T | ENSP00000508490.1:p.Arg177Trp | |
| ENST00000453231.6:c.550C>T | ENSP00000392197.2:p.Arg184Trp | |
| ENST00000535845.6:c.448C>T | ENSP00000437567.1:p.Arg150Trp | |
| ENST00000538924.7:c.529C>T MANE Select | ENSP00000438346.3:p.Arg177Trp | |
| ENST00000541910.6:c.294C>T | ENSP00000442681.1:p.Gly98= | |
| ENST00000642243.1:c.637C>T | ENSP00000494960.1:p.Arg213Trp | |
| ENST00000643817.1:c.487C>T | ENSP00000495610.1:p.Arg163Trp | |
| ENST00000644644.1:c.538C>T | ENSP00000494305.1:p.Arg180Trp | |
| ENST00000165698.9:c.529C>T | ENSP00000165698.5:p.Arg177Trp | |
| ENST00000437769.5:c.294C>T | ENSP00000401140.1:p.Gly98= | |
| ENST00000453231.5:c.550C>T | ENSP00000392197.1:p.Arg184Trp | |
| ENST00000490915.5:n.551C>T | ||
| ENST00000535845.5:c.448C>T | ENSP00000437567.1:p.Arg150Trp | |
| ENST00000538924.5:c.550C>T | ENSP00000438346.1:p.Arg184Trp | |
| ENST00000541910.5:c.294C>T | ENSP00000442681.1:p.Gly98= | |
| NM_001164730.1:c.550C>T , LRG_713t1:c.550C>T | NP_001158202.1:p.Arg184Trp | |
| NM_001164731.1:c.448C>T | NP_001158203.1:p.Arg150Trp | |
| NM_001164732.1:c.294C>T | NP_001158204.1:p.Gly98= | |
| NM_022912.2:c.529C>T , LRG_713t2:c.529C>T | NP_075063.1:p.Arg177Trp | |
| XM_005264502.1:c.529C>T | XP_005264559.1:p.Arg177Trp | |
| XM_005264504.1:c.415C>T | XP_005264561.1:p.Arg139Trp | |
| XM_011533043.1:c.550C>T | XP_011531345.1:p.Arg184Trp | |
| XM_011533044.1:c.511C>T | XP_011531346.1:p.Arg171Trp | |
| XM_011533045.1:c.505C>T | XP_011531347.1:p.Arg169Trp | |
| XM_011533046.1:c.550C>T | XP_011531348.1:p.Arg184Trp | |
| XM_005264502.2:c.529C>T | XP_005264559.1:p.Arg177Trp | |
| XM_011533045.2:c.505C>T | XP_011531347.1:p.Arg169Trp | |
| XM_017004725.1:c.550C>T | XP_016860214.1:p.Arg184Trp | |
| XM_017004726.1:c.550C>T | XP_016860215.1:p.Arg184Trp | |
| XM_017004727.1:c.550C>T | XP_016860216.1:p.Arg184Trp | |
| NM_001164730.2:c.550C>T | NP_001158202.1:p.Arg184Trp | |
| NM_001164731.2:c.448C>T | NP_001158203.1:p.Arg150Trp | |
| NM_001164732.2:c.294C>T | NP_001158204.1:p.Gly98= | |
| NM_001371279.1:c.529C>T MANE Select | NP_001358208.1:p.Arg177Trp | |
| NM_001371280.1:c.418-15581C>T | NP_001358209.1:n.418-15581C>T | |
| NM_022912.3:c.529C>T | NP_075063.1:p.Arg177Trp |